ADAMTS13 anticorps (AA 401-500) (Cy7)
Aperçu rapide pour ADAMTS13 anticorps (AA 401-500) (Cy7) (ABIN758897)
Antigène
Voir toutes ADAMTS13 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 401-500
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Réactivité croisée
- Humain, Souris
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Homologie
- Rat,Dog,Cow,Pig,Horse
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Purification
- Purified by Protein A.
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Immunogène
- KLH conjugated synthetic peptide derived from human ADAMTS13
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Isotype
- IgG
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anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) antibody
ADAMTS13 Reactivité: Humain WB, IF Hôte: Lapin Monoclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 299-488) antibodyADAMTS13 Reactivité: Humain, Souris, Rat WB, ELISA Hôte: Lapin Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 896-1131) antibodyADAMTS13 Reactivité: Humain WB, IHC, IP, ICC Hôte: Lapin Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 1328-1427) antibodyADAMTS13 Reactivité: Humain WB, ELISA Hôte: Souris Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 1300-1400) antibodyADAMTS13 Reactivité: Humain WB, IF Hôte: Lapin Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (C-Term) antibodyADAMTS13 Reactivité: Humain WB, ELISA, IHC Hôte: Lapin Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) antibodyADAMTS13 Reactivité: Humain WB, FACS Hôte: Lapin Monoclonal 23GB3925 unconjugated Recombinant Antibody
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) antibodyADAMTS13 Reactivité: Humain, Souris, Rat IF Hôte: Lapin Polyclonal unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 829-858) antibodyADAMTS13 Reactivité: Humain WB, IHC (p) Hôte: Lapin Polyclonal RB18029 unconjugated
anti-ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13) (AA 1328-1427) antibodyADAMTS13 Reactivité: Humain ELISA Hôte: Souris Monoclonal 4F12 unconjugated
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Indications d'application
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 μg/μL
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Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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Agent conservateur
- ProClin
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Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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Date de péremption
- 12 months
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- ADAMTS13 (ADAM Metallopeptidase with Thrombospondin Type 1 Motif, 13 (ADAMTS13))
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Autre désignation
- ADAMTS13
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Sujet
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Synonyms: Cleaves the vWF multimers in plasma into smaller forms. Von Willebrand factor cleaving protease, A disintegrin and metalloproteinase with thrombospondin mots 13, A disintegrin like and metalloprotease reprolysin type with thrombospondin type 1 mot 13, A disintegrin like and metalloprotease with thrombospondin type 1 mot 13, ADAM metallopeptidase with thrombospondin type 1 mot 13, ADAM TS 13, ADAM TS13, ADAM-TS 13, ADAM-TS13, ADAMTS 13, ADAMTS-13, ADAMTS13, ADAMTS13 protein, ATS13_HUMAN, C9orf8, TTP, von Willebrand factor-cleaving protease, vWF cleaving protease, vWF CP, vWF-cleaving protease, vWF-CP, vWFCP.
Background: This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motif) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene is the von Willebrand Factor (vWF)-cleaving protease, which is responsible for cleaving at the site of Tyr842-Met843 of the vWF molecule. A deficiency of this enzyme is associated with thrombotic thrombocytopenic purpura. Alternative splicing of this gene generates multiple transcript variants encoding different isoforms. [provided by RefSeq, Nov 2008].
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ID gène
- 11093
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UniProt
- Q76LX8
Antigène
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